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Presented by Jeff Mariner at the African Swine Fever Diagnostics, Surveillance, Epidemiology and Control Workshop, Nairobi, Kenya, 20-21 July 2011
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PENAPH
Participatory Epidemiology and the Use of Models to Design Control Strategies
c/o ILRI, P. O. Box 30709, Nairobi, 00100 Kenya; phone: +254-20 422 3000; fax:+ 254-20 422 3001; email:[email protected]
Participatory Epidemiology
The use of participatory rural appraisal techniques to collect epidemiological
knowledge and intelligence
Participatory Rural Appraisal (PRA)
• Qualitative intelligence gathering process
• Key informants• Problem solving
– Multiple methods– Multiple perspectives– Triangulation
• Best-bet scenarios
Existing Veterinary Knowledge
• Traditional terms and case definitions
• Clinical presentation• Pathology• Vectors• Reservoirs• Epidemiologic
features Photo: T. Leyland
Applications
• Basic Research • Active Surveillance
– Participatory Disease Surveillance (PDS)• Holistic Needs Assessment
– Stakeholders, livelihoods and risk• Impact Assessment
– Participatory Impact Assessment (PIA)– Qualitative and Quantitative
• Institutional change
Participatory Disease SurveillancePDS
• Active surveillance done by professionals
• Risk-targeted• High detection rate
– Information networks– Extended time frame
• Sensitive and Specific– Validation processes– Laboratory support
• Timely
Attributes of PE/PDS Programs
• Flexible approach that allows for discovery• Practitioners are problem-solvers and not enumerators• Strength of the approach lies in its flexible and qualitative
nature• Orients and complements, but does not replace structured
and quantitative methods• Information from diverse sources and methods• Analyzed in an iterative process referred to as
triangulation• Integrates biological testing and quantitative methods
when appropriate to objectives
PENAPHParticipatory Epidemiology Network for Animal and
Public Health
c/o ILRI, P. O. Box 30709, Nairobi, 00100 Kenya; phone: +254-20 422 3000; fax:+ 254-20 422 3001; email:[email protected]
• Nine core partners
•Building Surveillance Capacity
• Good Practice Guidelines
• Certification of Training
• Research, Policy and Advocacy
• Pro-Poor and One Health Focus
• Knowledge Exchange
Appropriate Combinations of Complimentary Techniques
• Participatory methods• Biological testing• Analytical methods
Persistence as a Function of Initial Herd Immunity
0
100
200
300
400
500
600
700
800
0 20000 40000 60000 80000 100000 120000 140000 160000 180000 200000
Initial Number Recovered (Immune)
Le
ng
th o
f O
utb
reak
(D
ays
)
Participatory Approaches to the Mathematical Modelling of
Rinderpest and CBPP
PARC, PACE and CAPE
Modelling Objective
• Model agents and lineages as they occurred in pastoral areas of East Africa
• Involve stakeholders at all levels in design and address principal questions of pastoralists and policy-makers– More useful and creates a sense of ownership
• Inform policy dialogue leading to more effective strategies– Targeting interventions and surveillance
Data Collection• Evidence-based literature review• Participatory epidemiology – expert opinion
– Mortality, prevalence, clinical course, spatial and temporal patterns and contact structure, estimation of R0
– SSI, proportional piling, matrix scoring, relative prevalence scoring, mapping and event trees
• Serology - Estimation of R0
“Some of us believe we have rinderpest, but we are not really sure. The disease looks like rinderpest, but it doesn’t kill the
animals. It is rinderpest-like or mild rinderpest.”
Somali elder on lineage 2 rinderpest
El Wak, Somalia 1996
Modelling Approach
• State-Transition• Stochastic
– Critical Community Size– Fade - Out
• Open Population• @ Risk Software• Input Parameters – Beta Pert Distributions• Single population and multipopulation• Outputs – Probability Distributions
E I RSb
μ μ μσμ
β γ α
α = recovery rateb = birth rateβ = effective contact rateγ = latency to infectious rateμ = non-specific mortality rateσ = RP mortality rate
S = SusceptibleE = ExposedI = InfectiousR = Resistant
RP Model Structure
ωr
ρ ωv
E I RSb
μ μ μσμ
β γ αr
Q
μ
V
αq
κψ
μ CBPP Model
The Basic Reproductive Number Ro
• Number of secondary cases resulting from one infected animal in susceptible population
• Ro is a feature of both the strain of infectious agent and the host population
The Importance of R0
• A measure of the transmission rate • Can be easily estimated from field data
– RP - Herd immunity threshold (1-1/R0)– CBPP - Average of first infection– HPAI – Final fraction size
• Effective contact rate, β, can be calculated from R nought.
• Herd immunity targets
Inter-Epidemic PeriodRinderpest in Sudan and Somalia
Temporal distribution of reports on rinderpest compatible events by year and interview area
So What?• Prevalence of Infection
– 0.1 – 0.2 %– Random clinical surveillance to OIE
standards (1%) not useful– Participatory disease surveillance
• Critical Community Size– ~200,000 head– Target vaccination to high risk populations– Large, remote pastoral communities
• Lineage 2 in Somalia– Modest herd immunity levels could
eradicate
Disease Persistence as a Function of the Initial Prevalence of Immunity
0
100
200
300
400
500
600
700
800
0 20 40 60 80 100
Initial Prevalence of Immune (%)
Days
Murle
Dinka
Toposa
Jikany Nuer
Lou Nuer
Jie
Niagatom
Gawere Nuer
Bor Dinka
Lotuko/Lopit
Laak Nuer
Boya/Didinga
Anuak
Kachipo
ProvincesRiversCattle Populations
300 0 300 600 Kilometers
N
EW
S
East Nile Cattle Populations
Traditional Livestock Exchange
Kachipo
1
2
3
Murle
Toposa
Jie
Heterogeneous RP Model for lineage 2 in the Somali Ecosystem
• Four populations• Multiple species
– Parameter values can set independently
• Eight year duration• Cattle and buffaloes• Buffalo R0 ~ 8
Four Sub-Population Epidemic Curves from a Heterogeneous Population Model for Rinderpest in Cattle Where the Between
Population Contact Rate is 1% of the Within Population Contact Rate
0
20
40
60
80
100
120
140
0 100 200 300 400 500 600 700
Days
Num
ber I
nfec
tious
Sub-population 1Sub-population 2Sub-population 3Sub-population 4
Results Over 2 Years
• Mean mortality 0.85% per year• 34% of iterations ended with a prevalence
of infection of 0.1 to 1%• Maximum prevalence 2%• Final average immunity 26%
Eight Year Model η = 0.005 and R = 35%
DurationMean 95th % Max Persistence
(%)
10,000 137 323 603 0
20,000 227 532 1100 0
30,000 329 878 1571 0
40,000 408 948 1915 0
50,000 477 1418 2633 0
100,000 1031 2553 2920 3
The Role of Buffaloes
Buffaloes % Immune
Cattle - Day of Last Case
Overall – Day of Last Case
5-15 245 247
15-25 264 269
25-35 261 266
45-55 258 265
55-65 253 260
Somali Ecosystem
• Buffalo act as an indicator host and do not contribute to persistence in cattle– Explosive outbreaks of short duration
• Small isolated communities can maintain Lineage 2 for prolonged periods
• Intensive surveillance and time
Potential of a Combined Vaccination and Treatment Strategy for CBPP
Scenario Baseline 1/α 75% 1/α 50% 1/α
None 75.4 178 59.6 129 33.2 64
Annual – 5 yr 67.8 130 43.0 79 7.6 24
Biannual – 2 yr 57.2 129 - - 4.4 20
Biannual – 5 yr 35.2 83 8.0 43 0.4 16
Indications from the CBPP Modelling
• Eradication not possible with existing vaccine without severe movement control
• The potential impact of treatment is at least great as available vaccines– Private sector and consumer driven application
• Research on treatment regimes merits the same level of attention and investment as vaccine development.
Conclusion
• Simple, intuitive models serve as good communications tools for underlying concepts
• Bring diverse information together to be tested as for biological coherence
• Choose between strategy options or identify new options
• Involve beneficiaries and decision-makers from the outset.